The Association of Ophiothrix lineata and Callyspongia vaginalis: A



The Association of Ophiothrix lineata and Callyspongia vaginalis: A
P. S. Z. N. I: Marine Ecology, 5 (1): 9-27 (1984)
0 1984 Paul Parey Scientific Publishers, Berlin and Hamburg
ISSN 0173-9565/InterCode: MAECDR
Accepted: 12.5.1983
The Association of Ophiothrix lineata
and Callyspongia vaginalis; A BrittlestarSponge Cleaning Symbiosis?
Smithsonian Oceanographic Sorting Center, Smithsonian Institution, Washington,
D . C., 20560, U.S.A.
With 7 figures
Key words: Ophiothrix lineata, Caflyspongia vaginafis, brittlestar, echinoderm, sponge,
symbiosis, predation, periodicity, feeding.
Table of contents
10 Problem
10 Material and Methods
10 1. Location
12 2. Elapsed-time cinematography
12 3. Behavioral analyses
13 4 . Size and distribution of brittlestars
13 5. Predation
13 Results
13 1. Distribution of brittlestars
14 2. Circadian rhythm
14 3. Feeding activity
18 4. Fish predation
19 5. Regeneration
19 Discussion
19 1. Obligate commensalism
19 2. Sponges as a refuge from predation
22 3. Sponges as a source of food
24 4. Speculation regarding a cleaning symbiosis
25 Summary
25 Acknowledgements
25 References
Abstract. The relationship between a sponge, Callyspongia vaginafis, and an associated brittlestar,
Ophiorhriv Zineafa, was examined for mutualistic symbiotic interaction. Cinematography, feeding
experiments, and analyses of stomach contents reveal that 0. lineata (unlike other Ophiothrix
species) is a non-selective deposit feeder. Its diet consists of detrital particles adhering to the sponge,
which are too large to be utilized by the sponge as food. Thus, the brittlestar cleans the inhalent
surface of the sponge as it feeds. Since siltation interferes with sponge pumping-activity, it is
suggested that the cleaning behavior of 0. lineara may enhance the filtration capability of C.
vaginafis. in situ elapsed-time films show that brittlestars expose their arms when they feed,
suggesting that they feed only at night because of a need to avoid diurnal predators. Manipulative
experiments show that residence in C. vaginalis protects 0. lineafa from predatory fish. A
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comparison of the incidence of arm regeneration for brittlestars residing on C. vuginalis, and on a
toxic sponge, Neofibularia nolitungere, indicates that factors other than sponge toxicity are involved
in protecting sponge-dwellingbrittlestars.
According to WESTINGA
(1981, p. 149) the fauna inhabiting sponges
is “an ecological community, in which, however, interrelationships are not yet
clear.” Brittlestars are a common component of that community. Their a:jsociation with sponges has been documented in the scientific literature (WCGINMTE
1949; PEARSE, 1950; HYMAN,1955; BACESCU,
1971; R i h z L E R ,
1975) and by the popular press (MURPHY,
1980; SEFTON,
1982). In some cases the
association is facultative or fortuitous and the brittlestars involved may be found
on or off the sponge. The association of Ophiothrix quinquemaculata (DELLE
with sponges, for example, has been attributed simply to the climbing
behavior of the brittlestar or its reaction to water currents (FEDRAet al., 1976;
1980). Unfortunately, the ecology of brittlestars
which are facultatively associated with sponges has not been investigated in
sufficient detail to accurately characterize the interactions between brittlestar
and sponge (PEARSE,
1950; WURZIAN,
In cases where the two taxa are invariably associated there may be a strict
symbiosis, with at least the brittlestar benefiting from the association. The
brittlestar Ophiothrix lineata LYMAN,for example, has been reported as an
associate of various sponge species. This study examines the interaction of 0.
Zineatu with a sponge, Callyspongia vuginulis (LAMARCK),
to clarify the nature of
the symbiosis between the two organisms.
It is possible that sponges offer the brittlestar a refuge from predation. To
better understand this potential interaction an additional sponge species was
investigated. Neofibularia nolitangere (DUCHASSAING
~ ) chosen
since it is considerably more toxic than Callyspongia vuginulis, and it lharbors
several of the same brittlestar species as C. vaginafis. Toxicity cciuld be
evaluated as a factor in protecting sponge-dwelling brittlestars, by comparing
the physical condition of brittlestars associated with the two species of sponges.
The diet and mode of feeding of Ophiothrix lineata were studied to determine
whether it uses the sponge as a source of food. Additional complexities of the
association were considered. For example, I indicate below that Cullyspongiu
vaginalis may benefit because 0. lineata clears debris from the incurrent surface
of the sponge host and might thereby enhance the filtering efficiency of the host.
Material and Methods
1. Location ’
The study site was a cut in the Belize Barrier Reef to the south of Came Bow Cay ( P ~ ~ Z L&E R
1982, p. 11, for location). The area is about 5 m deep, predominantly a sandy bottom
with scattered coral heads, sponges, gorgonian colonies, and patches of seagrass. It is subjected to
strong tidal and wind-driven currents that can dramatically alter the turbidity of the water in the cut.
Fig. 1 (right). At night, the arms of the brittlestar,
Ophiothri* lineata, are extended along the outer
walls of the sponge, Callyspongia vaginalis. Polyps
of the epizoic zoanthid, Pnrazoanthus parasiticus
& Mrcm~orrr)are evident on the
largest sponge tube.
Fig. 2 (bottom). At night, the distal portion of the
arms of 0phiorhri.x lineata protrude from the osculum of Callyspongia vaginalis. As the brittlestar’s
arms slowly sweep across the inhalent surface of the
sponge its attenuate tube-feet and long, slender
arm-spines collect the detrital particles on which it
Fig. 3 (right hand bottom). A tube of Callyspongia
vaginnlis tom open during the day to reveal a
specimen of Ophiothrix lineata. The brittlestar’s
disc is covered by fields of low, rough granules
alternating with large, bare radial shields. The lines
from which the species name derives are visible
along the dorsal surface of the arms.
2. Elapsed-time cinematography
A tube sponge, Callyspongia vaginalis, with a resident population of the brittlestar, Ophiothrix
lineata, was filmed in situ for three days using an underwater strobe and a 16mm elapsed-time movie
er al.,
camera set for exposures at 20sec intervals (equipment described in detail by EDGERTON
1968). A buoyant plastic float, used as a current meter, was tethered near the b3se of the colony
inside the picture area. The angle of the float line indicated approximate current :<peed(HENDLER,
1982 a), however, only relative fluctuations in current speed are considered in this paper.
During filming, the intensity of ambient illumination was monitored continuously with a
photometer (United Detector Technology, Inc. 40 X Opto-meter) and a potentiometric strip chart
recorder. The photometer sensor was shielded with an uncalibrated diffuser and mounted on an
unshaded sector of the laboratory roof on Carrie Bow Cay.
3. Behavioral analyses
Using the time-lapse Nm, the movements of the brittlestars and the rates of sediment clearance
from the surface of the sponge were analysed with a stop-motion 16-mm projecror (L-W Internahonal224-A MK VI Photo-Optical Data Analyser). Brittlestar activity was meascred by enumerating the brittlestar arms visible-on the outer (inhalent) surface of the sponge at appropriate intervals
. - 1, 2, 3).
To evaluate the rate at which adhering material was removed from the surface sf the sponge, the
sponge was dusted with fine sediment before the nocturnal cycle of brittlestar activity and then
filmed. Frames of the film were projected and traced on graph paper, and the area covered by
sediment in each frame was estimated by counting graph paper squares. The clearance rates wer2
calculated separately for portions of the sponge that were reached by the brittlestar arms and for
portions unaffected by the movements of the brittlestars. These results contrast the rate of clearance
effected by the brittlestar with the rate of clearance atttributable to gravity and water movement.
To clanfy whether brittlestars merely dislodged particles from the surface of the sponge or
actually could ingest them, the following experiment was performed. A mixture of brine shrimp
eggs, and chopped fish scales and mucus was applied to the surface of a sponge. The eggs measured
0.47 k 0.03 rnm (X k s. d.) diameter. After 15 min, the sponge tubes were quickly ':om open (Fig. 3),
the brittlestars were removed, and while still underwater they were put into a plastic bag that was
injected with concentrated formaldehyde solution. This treatment ensured that the stomach
contents were quickly preserved and that the brittlestars did not regurgitate. Afti:r transferring the
preserved samples to alcohol, the gut contents were removed from the brittlestar discs and examined
for the presence of brine shrimp eggs.
The constituents of the natural diet of Ophiothrix lineata were determined for !)O specimens from
14 Callyspongia vaginah sampled during the afternoon and for 71 specimens from 11 sponges
sampled at night. The specimens were preserved in the same manner as those in the brine shrimp
ingestion experiment. Stomach contents from each specimen were rinsed into a vial. When particles
in the vials settled, all the samples were scrutinized. The quantity of material in each sample was
rated on a scale from 1 to 3, based on the relative volume of material in the sample.
After gently agitating the sample vial, a subsample of the gut contents from e , x h individual was
removed with a wide bore pipette and placed on a well slide beneath a coverslip. A single, randomly
chosen microscope field at 100 x magnification was traced using a camera lucida, and the longest
axis of each particle in the field was measured from the drawing. The frequen'zy distributions of
particles in the stomachs of brittlestars sampled during the day and of those sampled at night were
calculated (for 0.05 mm size categories) as a percentage of the total number of particles measured.
The naturally occurring accumulation of particles on the outer surface of Caliyspongia vaginalis
was sampled for comparison with the brittlestar stomach contents. An underwater suction device
1971), fitted with a 54pm mesh screen over the exhaust valve, was used to capture material
clinging to the incurrent wall of the sponge. Collections were made in the afternoon from 20 sponge
colonies, and the settled particles in the sample were analysed microscopically and statistically using
the same techruque applied to the stomach contents.
Brittlestar-sponge symbiosis
4. Size and distribution of brittlestars
The populations of brittlestars on 12 specimens of CalZyspongia vaginafis and 6 specimens of
Neofibufuria nofitungere were removed underwater. For C. vaginalis, every brittlestar visible on the
outer wall of the sponge was collected first. Then, the tubes of the sponge colony were opened and
the brittlestars within were placed in a separate container. Because of the complex structure of N .
nolitangere, the brittlestars collected from the outside and inside of each colony were combined.
The specimens collected in the field were anaesthetized and preserved in alcohol in the
laboratory. After identifying each brittlestar to species, the disc diameters and maximum arm
lengths were measured with calipers, ruler, or ocular micrometer. In addition, the arms of each
specimen were examined for signs of autotomy or breakage and regeneration. A regeneration index
(RI) was calculated as the fraction of regenerating arms divided by the number of arms examined,
multiplied by 100. Arms broken during sampling were disregarded since they could not be critically
examined for signs of regeneration.
5. Predation
The degree of protection afforded the brittlestars by Callyspongia vaginalis was evaluated in 10
experiments, as follows. A sponge was selected for the experiment with a resident population of
Ophiothrix lineuta. Eleven specimens of 0. linearu were removed from another sponge. Five of
those brittlestars were placed on the sand at the base of the experimental sponge, and five were
placed on the outer wall of the experimental sponge. Finally, one specimen was crushed to attract
predators. Attacks by fish that damaged brittlestars beneath, on, and inside the experimental
sponge were tallied separately. To determine the percentage of survival after 5 min, the number of
0. lineata remaining on and beneath the sponge were counted. The experimental sponges were not
examined to determine the number of resident brittlestars in the sponge tubes, because specimens
inside the sponge were never attacked.
A related series of 10 experiments was carried out, by placing crushed specimens of 0. liiieafu
inside 3 to 5 tubes of a sponge and then an additional crushed specimen on the sand at the base of the
sponge. Predatory fish attracted to the area were observed to determine whether they would pursue
and attack injured brittlestars inside the sponge.
1. Distribution of brittlestars
Different suites of brittlestar species are found on Caffyspongiavaginafis and
Neofibularia nofitangere. Fig. 4 shows that 6 species of brittlestars are associated
with the two sponges. However, Ophiothrix fineata and 0. oerstedi LUTKENare
is restricted
restricted to C. vaginafis, while Ophiactis quinqueradia LJUNGMAN
to N. nofitangere.
Populations of certain brittlestars show different characteristics on the two
sponges studied. There are differences in the mean size of the Ophiothrix
angulata (SAY)and 0. suensoni L ~ K EonNthe two species of sponges (Fig. 4).
For both brittlestar species the mean disc diameter of specimens on Neofibufaria
is significantly greater than for specimens on Callyspongia (0. angulata, t =
72.52, n = 130, P < 0.001; 0. suensoni, t = 19.45, n = 142, P < 0.001).
The differences in the mean sizes of 0. fineatu inside and outside Caffyspongia vaginafis is more striking, with larger specimens inside, and is also statistically significant (t = 16.34, n = 154, P < 0.001) (Fig. 4). 0. angulata shows the
same trend (t = 2.40, n = 103, P < O.OZ), as does 0. suensoni (t = 5.46, n = 7 5 ,
P < 0.001) (Fig. 4). The data for 0. oerstedi are inadequate to test for such a
difference in mean disc diameter.
2. Circadian rhythm
A specimen of Callyspongia vaginalis was filmed for three days and the patterns
shown in the three films were quite similar. The results of the film taken on 19
April, 1982 are shown in Fig. 5. The activity of the brittlestar arms outside the
sponge (Figs. 1, 2), begins at dusk and diminishes in the morning. The peak
intensity of activity occurs between about 1900 and 2400 h, during darkness.
Because there was moonlight during the filming period, photometer values for
illumination were recorded at night. There is no evident correlation between the
intensity of nocturnal illumination and the activity of brittlestars (Fig. 5 ) .
Neither is there an obvious correlation between the strength of the current
(generally travelling in surges moving less than 5 cm s-I) and the activity of the
brittlestars (Fig. 5 ) .
3. Feeding activity
The nocturnal behavior of Ophiothrix lineafu consists of moving its arms like a
pendulum, very slowly sweeping across the surface of the sponge (Figs. 1, 2).
Fig. 4. Size-frequency distributions of brittlestars (Ophiofhrixlineafa, 0. suensoni, 0. angulafa, 0.
oersfedi, Ophiactis savignyi (M. & T.), and 0. quinqueradia) collected from the outside and inside
surfaces of Callyspongia vaginalis, and from Neofibularia nolifangere. The disc diameter (mean and
s. d.), number of specimens, and regeneration indexare indicated for each sample of brittlestars.
Brittlestar-sponge symbiosis
The tip of the arm moves at a mean rate of 3.14 k 1.96 cm/min. Only 1.6 % of
the 2,566 arms counted during film analysis were lifted off the incurrent wall of
Callyspongiu; most arms remain in contact with the sponge (Fig. 5).
When the outside of a sponge was dusted with sediment, the moving arms of
the brittlestars cleared a swath through the film of sediment clinging to the
sponge. Fig.6 illustrates the fraction of the surface of the sponge cleared at
intervals after the brittlestars began feeding in the evening. The sediment on the
sponge disappears in step with the emergence of brittlestar arms and increasing
brittlestar activity (Fig. 6). Comparing the portion of the sponge brushed by the
moving brittlestar arms with that area outside the reach of the brittlestars,
clearly the portion of the sponge affected by the brittlestars loses silt more
rapidly than the remainder of the sponge (Fig. 6).
2 40
. . '..... ..
. . .... .' .....
.. - ..
.... .. . ..... .. .. .. . . . ..........
.. ..-.
. . .
. . . . . . . . . . . . . ....................
TIME [h]
Fig. 5. Fluctuations of the intensity of activity of Ophiothrix lineata on Callyspongia vaginalis,
expressed as the number of brittlestar arms visible on the outside surface of a sponge (large solid
circles) in an elapsed-time film. Also shown are: the numbers of arms lifted off the surface of the
sponge (open circles), the relative light intensity (squares), and the angle of the current-meter float
(small circles).
. * *
* * *
* .
* .
* *
.. . .
, ,* : f ' . . ' ,
. . . . . .
. . . -
. . . . .
T I M E [min]
Fig. 6. The rate of clearance of sediment from the surface of a specimen of Callyspongin vaginalis
dusted with silt, measured from elapsed-time films for two nights. The rate of clearance csn portions
of the sponge reached by Ophiofhrix fineafa (circles) is contrasted with clearance rate for the area
not swept by brittlestar arms (squares). The number of 0. lineata arms visible on the sponge
(asterisks) is directly proportional to the intensity of brittlestar activity.
An experiment utilizing brine-shrimp eggs was performed to determine
whether the particles removed from the surface of Callyspongia vaginalis are
merely brushed off the sponge or could be ingested by the brittlestars. Of 14
Ophiothrix lineata exposed to the brine-shrimp egg mixture during two night
dives, 7 individuals ingested brine-shrimp eggs. Four specimens of 0. lineata
were exposed to the mixture during the day, and no brine-shrimp eggs were
found in their stomachs. These data are too few to warrant formal seatistical
comparison of night versus day behavior. In the stomach contents of 12
specimens collected at night, there was naturally occurring food material, the
remaining 2 specimens had empty stomachs. In contrast, 1 specimen from the
day sample contained naturally occurring food and 3 lacked food. These data
are consistent 'with the cinematographic record of greater feeding activity at
night and the results, discussed below, of an analysis of naturally occurring
stomach contents.
Brittlestar-sponge symbiosis
It was rarely possible to discern identifiable particles amongst the material
sampled in stomach contents and material sampled from sponges. The samples
consisted largely of unidentifiable debris. Some chitinous parts, diatoms, bits of
plant tissue, and sponge spicules regularly appeared in small numbers.
Foraminifera, fragments of filamentous algae and strands of blue-green algae,
copepods, ostracod fragments, gorgonian spicules, and tiny gastropods were
occasionally or rarely detected in the stomach contents and from the sponge
wall. In addition, fragments of thecate hydroids were collected from the surface
of the sponge.
T o determine whether the brittlestars selectively removed material from the
surface of the sponge, the size frequency distributions of particles from the
sponge surface and from the stomach content samples were compared (Fig. 7).
The same range of particle sizes occurs on the sponge and in the brittlestar
stomachs from night and day collections. Pairwise in the three samples, the
proportions of particles in different size categories are not significantly different
(x’ = 1.0067 with d.f. = 10, P = 0.9995). This result suggests that the
brittlestars do not remove material selectively, at least according to particle size.
One has to consider that the size spectrum in the stomach may have been
influenced by agglutination or breakdown of particles by the brittlestar and the
technique of removing particles from the sponge. However, the similarity of the
size-frequency distributions from the three groups is striking.
cO.05 ~0.10~0.15 cO.20 ~ 0 . 2 540.30 ~ 0 . 3 5~ 0 . 4 0~ 0 . 4 5~ 0 . 5 020.50
Z0.05 20.10 20.15 Z0.20 E0.25 20.30 Z0.35 ’0.40 20.45
Fig. 7. Comparison of the size-distributions of particles: siphoned off the surface of Callyspongia
vaginalis (number of particles = 1,369), removed from the stomachs of Ophiothrix lineata sampled
during the day (n = 499), and removed from the stomachs of 0. tineara sampled at night (n =
It is noteworthy that although the food-particle size distribution is similar for
the stomach contents of brittlestars during the day and at night, only 21 % (n =
91) of the brittlestars were feeding during the day compared to 86 % (n := 71) at
night. This difference in the incidence of full and empty stomachs in day and
night samples is significant (FISHER'SExact Test: n = 162, P < 0.001). The
volume of material in the stomachs of animals sampled at night was compared
with that in the stomachs of animals collected during the day, by ranking the
volume of material from 1 (low volume) to 3 (high volume). For night samples
the number of spccimens showing values 1 , 2 , and 3 is, respectively, 28,21, and
12. For the day samples there is a lower volume of stomach contents per
specimen, with 18, 2, and 0 individuals in the same categories. Moreover, the
hypothesis that the occurrence of the three ranks was the same in the night and
day samples is rejected (x' = 12.2568 with d. f. = 2, P = 0.0027). Thus, more
brittlestars feed at night and their volume of stomach contents is greater than
that of day-specimens.
4. Fish predation
Attacks on brittlestars in the lumen of Caflyspongia'vaginalis, and those placed
experimentally on t h e outside of the sponge, and on the sand beneath the
sponge were analysed. At night, potential predators on brittlestars, such as
hermit crabs, squirrelfish, and grunts were present. However, these predators
did not approach the experimental sponges or attack Ophiothrix lineata. During
the day, fish reached the experimental sponges within 3 to 112 SIX. The
predominant species were Hafichoeres bivirtarus (BLOCH),Halichoeres garnotfi
and Scarus croicencis BLOCH.Other fish attracted,
with much lower frequency, were Sparisonza chrysopterum (BLOCH&
Cafamus bajonado (BLOCH& SCHNEIDER),
2nd Thalassoma bifusciatum (B LOCH).
Marauding fish more frequently attacked brittlestars that were on the sand
than those that were on the exterior of sponges (48 versus 18 attacks), and the
survival of brittlestars on the sponges was higher than for those on the ground
(82% versus 64%). In the experiments, Ophiothrix lineata living within the
sponges were never attacked by fish. The brittlestars on the sponge and on the
ground exhibited frenzied movements that probably intensified attacks by fish
and increased the mortality of brittlestars in the experiments.
In another series of experiments, comparing fish attacks on injured GI.lineafa
beside Caflyspongia vaginafis, versus attacks on injured brittlestars within the
sponge tubes, confirmed the effectiveness of the protection provided by the
sponge. Fish attacked the brittlestars on the bottom within 4 to 102 sec, but fish
did not molest the individuals in the sponge, even when the arms of injured
brittlestars protruded from the osculum.
The film record shows that most of the fish in the study area were present
during the day. Between 0530 and 0800 h, when brittlestar activity virtually
ceased, 61 fish were counted by observing a film frame for every 6 min interval.
Using the same sampling interval only 9 fish were counted over the much longer
period from 1830 to 0530 h. Thus, fish were recorded in greater numbers during
Brittlestar-sponge symbiosis
the day. The diurnal and nocturnal fish populations were composed of different
species. At night, mostly squirrelfish and grunts were filmed, but during the
daytime predominantly wrasses, parrotfish, and damselfish were recorded. The
latter 3 taxa attacked brittlestars in the predation experiment.
5. Regeneration
Regeneration indices (RI) are tabulated in Fig. 4; higher values indicate higher
frequency of autotomy or breakage and regrowth. Ophiothrix lineata specimens
from the lumen of Callyspongia vaginalis have a higher RI value than specimens
collected from the outer surface of the sponge. The same trend is shown by
Ophiothrix angulata. Notably, Fig. 4 also shows that brittlestars on the outside
of the sponge are considerably smaller than brittlestars on the inside.
The RI values of brittlestars were compared between populations from
Callyspongia vaginalis and Neofibularia nolitangere to gauge the relative degree
of protection provided by the two species of sponges. Ophiothrix suensoni has a
higher RI value on Neofibularia than on Callyspongia, but 0. anguluta has a
lower R I value on Neofibularia than on Callyspongia. Interestingly, Ophiothrix
suensoni and Ophiothrix anguluta both are generally of larger size on
Neofibularia than on Callyspongia (see Fig. 4 and “Distribution” - Results
1. Obligate commensalism
(1955, p. 687) noted that for brittlestars “Their small size and flexible
arms fit them for clinging to other animals, especially branching types, and
hence it is not surprising that they often occur in association with sponges and
coelenterates”. Despite their obvious morphological specializations for occupying large, sessile organisms, the adaptive value of such associations for the
brittlestars and sponges is not well understood. Fortunately, it is possible to
gauge the significance of the dependence by observation and experiment on
brittlestars requiring sponge hosts.
It appears that Ophiothrix lineata invariably is associated with sponges.
(1977) suggested that the presence of 0. lineata was
governed by the availability of suitable sponges, an observation supported by
other investigations (CLARK,1933; DEVANEY,
1974). In contrast, the other
brittlestar species that live on the same sponges as 0. lineata, live on substrata
besides sponges as well (CLARK,1933; DEVANEY,
1977). These findings support the hypothesis that 0. Zineara is an obligate
commensal of sponges.
2. Sponges as a refuge from predation
Abundant evidence has been published showing that brittlestars suffer heavily
from predation. RANDALL
(1967) reported on 33 species of Caribbean fish that
feed on brittlestars. They occurred in more than 10 % of the stomach content
samples for 10 fish species. He found that Ophiothrix was the most common
brittlestar genus identified from fish stomach contents, at least in part because
the spines of Ophiothrix species are so easily recognized. Of the 10 fish species
referred to for which brittlestars are an important dietary component, 6 fed on
Ophiothrix. Those include 3 diurnal wrasses, Bodianus rufus (L.) , Halichoeres
2 porgies, Calamus calamus
garnotti, Halichoeres poeyi (STEINDACHNER);
Calamus pennatufa GUICHENOT,
and the nocturnal
grunt, Anisotremus virginicus (L.). Another wrasse, Thalassorna bifa.i.ciatum,
which also ingests Ophiothrix may consume a diet of 30.8 % brittlestars (FEDDERN,1965; RANDALL,1967).
There is no evidence of a guild of fish that feed primarily on sponge-dwelling
brittlestars, though there is a group of fish which prey largely on sponges
1968). Only one of the fish that feeds on sponges,
Cantherhines pullus (RANZANI),has been found to ingest brittlestars, and
Ophiothrix spp. were found in its stomach contents (RANDALL,
1968). Certain fish may occasionally feed on both sponges and
brittlestars. For example, BEEBE& TEE-VAN(1928) reported some sponge
material in the guts of Halichoeres radiatus (L.), a fish that feeds on brittlestars
1967). Both brittlestars and sponges are a minor component in the
diets of the fishes Anisotremus surinarnensis (BLOCH)and Haemulori album
1967). In European waters crustacean
predators that attack Ophiothrix quinquemaculata associated with sponges
include the crab Pilumnus hirteffus (L.), the hermit crab Paguristes oculatus
(FABR.),and the spiny lobster, Palinurus vulgaris LATR. (VASSEROT,
1979, 1980).
There is ambiguous evidence in the literature regarding whether brittlestars
are protected from predation by their association with sponges. The potential of
the sponge as a physical barrier to predation is obvious. In addition, fish might
avoid the toxins or noxins (noxious compounds) synthesized by sponges. BAKUS
& THUN(1979) reported that 57 % of the Caribbean sponge species tested were
toxic to fish. Neofibularia nolitangere causes intense pain and dermatitis when
handled by humans, and it is strongly toxic to fish (BAKUS& THUN,1979).
Callyspongia vaginalis was reported by HALSTEAD
(1965) to be toxic to fish, but
BAKUS& THUN(1979) found that the species liberated noxins that were not
lethal to the fish they tested. Not surprisingly, sponge-eating fish feed more
often on C. vaginalis than on N . nolitangere (RANDALL
However, perhaps because of their chemistry and the presence of spicules in
many species, sponges are generally not an attractive food source for most fish.
(1968) concluded that, overall, sponge-eating fish are of
little importance in controlling populations of Caribbean sponges.
Considering the contrasting effects on fish of toxins from the two sponges,
Calfyspongia vaginalis and Neofibularia nolitangere, it would be expected that
brittlestars associated with the latter, distasteful species would show less damage
from predation. However, the results of the regeneration index measurements
of brittlestars on C. vaginalis and N . nofitangere were equivocal on this point,
perhaps because of the inadequacies of the RI as an index of predation. While
the incidence of arm regeneration may parallel the intensity of predation, it is
Brittlestar-sponge symbiosis
not necessarily directly related to fatal encounters. Brittlestar species that are
not ingested by fish can still exhibit a considerable amount of arm regeneration
(SHIRLEY,1982). Moreover, regeneration index values are probably biased by
the differing regenerative abilities of particular brittlestar size classes and
The trends in R I values for particular brittlestar species on Callyspongia and
Neofibularia were inconsistent. This implies that factors other than sponge
toxicity may be involved in the intensity of predation directed at brittlestars on
various sponge species. It is possible that the presence or absence of brittlestar
species on certain sponge species (Fig. 4) is related to brittlestar requirements
for such factors as sponge morphology or microhabitat.
The more straightforward data of the fish predation experiments show that
Cullyspongia vaginalis offers Ophiothrix lineata protection from fish. Mortality
from fish attacks increases for brittlestars inside sponges, over those placed on
the outside surface of sponges, to those placed on the substratum near sponges.
These results, and evidence of regeneration of 0. lineata on C. vaginalis,
indicate that the brittlestar normally suffers a degree of predation while on the
sponges. It appears (somewhat unexpectedly) to be the larger individuals, which
extend their arms outside the sponge only a t night, that are most seriously
affected by predators. The small specimens (both 0. lineata and 0. angulutu),
primarily found on the outer wall of the sponge, show less evidence of
regeneration. If this observation is not a technical artifact (a product of the
difficulty of identifying damage and regeneration in small specimens), it is likely
that the tiny specimens on the outside of the sponge simply are not detected by
visual predators. Certainly, they are not easily seen by the human observer,
because of their small size and their pale coloration.
In addition, the occurrence of small individuals outside the sponge and large
individuals inside the sponge suggests that there may be settlement and recruitment of Ophiothrix lineata, 0. angulata, and possibly even 0. suensoni on the
outside of Callyspongia vaginalis. Subsequently, larger specimens may take
residence inside the sponge. However, it is also possible that competition or
other negative interactions between size classes (or species), or the activities of
predators results in the observed distributions.
Since Ophiothrix lineata is a detritus feeder its circadian cycle is likely not a
function of the periodical availability of its food, as detritus is generally in
constant supply. Rather, the circadian feeding pattern detected with elapsedtime cinematography is probably related to the damage inflicted by predators on
the larger specimens of 0. lineatu. The results of several studies on echinoderms
suggest that nocturnal activity is a predator avoidance tactic (references in
NELSON& VANCE(1979) demonstrated experimentally that the sea urchin,
Centrostephanus coronatus (VERRILL)
, which is normally active only at night, is
preyed upon by fish when exposed in daytime experiments. The results of the
predation experiments using Ophiothrix lineata were analogous. The greater
abundance of diurnal than nocturnal predators shown in the elapsed-time film
suggest that the brittlestar’s circadian rhythm is an adaptation for predator
avoidance. Interestingly, the Mediterranean species, Ophiothrix p i n quernaculata, sometimes a facultative associate on sponges and sometimes
found in dense monospecific aggregations, maintains its feeding posture continuously rather than hiding during the day. Individuals of 0. quinquemaculata
only shift position in response to changing current or to direct disturbance by
1979). The sort of circadian
predatory benthic invertebrates (FEDRA
behavior shown by 0. lineata on Callyspongia vaginalis would be nonadaptive
for 0. quinquemaculata because 0. quinquemaculafa does not associatto with a
permanent host which provides a refuge from predation.
A problem with this interpretation of the nocturnal activity pattern of
Ophiotlzi-ix lineata (as an escape from predation) is that certain fish wh:,ch prey
on Caribbean Ophiothrh spp. are active at night as well as during the day. For
example, the nocturnal porkfish (Anisofrernus virginicus) preys on brittlestars
(1979) found that in the North Adriatic Sea,
the brittlestar-eating hermit crab, Paguristes oculatus, is more active during
daylight hours than after dark. However, brittlestar-eating pagurids in the
Caribbean, such as Petrochirus diogenes L., feed nocturnally (unpubl. obs.).
These inconsistencies must be weighed against the observation that the diurnal
wrasses were the most important group of brittlestar-predators reported by
(1967) and were the dominant predators in the predation experiments
discussed in the present paper. Evidently, the diurnal crypsis of Ophiothrix
lineata enhances the survival of the species.
3. Sponges as a source of food
(1982, p. 168) wrote that “All members of the genus Ophiothrix so far
studied - 0. quinquemaculata, 0. spiculata, 0. angulata, and 0. fragiiis - are
specialized suspension feeders”. For example, Ophiothrix fragilis (ABILDGAARD)
raises its arms in moderate currents and unselectively ingests particles of
suspended material that adhere to the tube feet and spines of its arms (WARNER
1975). In fact, the elevation on sponges of the closely related
Ophiothrix quinquemaculata has been estimated to provide the filter-feeding
brittlestar a threefold increase in availability of suspended food particles
The feeding mode of Ophiothrix lineata differs fundamentally from that of its
congeners. The combined observation of arm movements of Ophiothrix lineata
on the surface of Callyspongia vaginalis, and their ingestion of particles (i. e.,
brine-shrimp eggs) on the surface of the sponge, indicate that 0. lineata is a
deposit feeder. This conclusion is also affirmed by the similar nature and the size
distribution of particles on the surface of the sponge and in the stomachs of the
brittlestars. In addition, 0. lineata maintains its arms in contact with the sponge,
whereas filter-feeding brittlestars characteristically project their arms into the
(1977) were
water above their substratum. Apparently, KISSLING
mistaken in supposing that 0. lineata (because of its arm morphology) filterfeeds.
In the association between Callyspongia vaginalis and Ophiothrix finesrta, the
sponge provides the brittlestar with detrital material and a suitable surface from
which to feed. The brittlestar ingests, for the most part, unidentifiable particles
of debris, although several taxa of animals and plants are observed in the
Brittlestar-sponge symbiosis
brittlestar stomach contents. The observations of the brittlestar’s pattern of
activity, the contrasting proportion of animals feeding during day and night, and
the fluctuations in the volume of stomach contents, all indicate that feeding is
primarily a nocturnal behavior.
T h e dependence of Ophiothrix lineata on Callyspongia vaginalis for food is
clear evidence for a commensal relationship. Ophiothrix lineata could be
regarded as a parasite if its food were of value to the sponge, but several lines of
evidence indicate that brittlestars do not collect material which can be utilized
by sponges. For example, Ophiothrix fragifis responded to both phytoplankton
and 60-90 p m particles of radioactively labelled detritus, but under the same
experimental regime, three species of sponges showed relatively low uptake of
labelled detritus (BEVISS-CHALLINOR
& FIELD,1982).
Brittlerstars are clearly capable of feeding on particles larger than those
readily accessible to digestion by sponges (HENDLER,
1982 b). Brittlestar digestion is extracellular, mediated by enzymes secreted into the lumen of the
stomach. Particles, reduced to suitable size by extracellular digestion, are
absorbed through the stomach lining by pinocytosis (PENTREATH,
1978). On the other hand, detrital particles
accounted for only about 3 % of the microscopically resolvable, particulate,
organic biomass available as food to sponges (REISWIG,1971a). Seemingly.
much of the material ingested by brittlestars is detritus, unavailable to sponges
as food.
The incurrent flow of dernosponges traverses several filter systems including
pores in the dermal membrane, inhalent canals, prosopyles, and choanocyte
collars (references in REISWIG,
1971 a). The size of the opening in these filters
restricts the upper size limit for particles taken by the sponge. In Calfyspongia
diffusa (RIDLEY),
incurrent pores in the dermal membrane are 50pm, and major
incurrent canals from subdermal spaces open into lacunae around choanocyte
chambers via 25 p m apertures. The prosopyles are 1p m triangular spaces
between choanocyte cell bodies. The size of the pores in the dermal membrane
dictates an upper limit of 5 0 p m for particles entering the sponge and particles
between 1 and 5 0 p m in size must be phagocytized outside the choanocyte
1982). The parameters for C. vnginnfis are
chambers (JOHNSTON
probably similar to those for C. diffusa (RUTZLER,pers. comm).
REISWIG(1971 a) found that most of the food of sponges was small enough to
be phagocytized by the choanocytes. He characterized 95 % of the total plankton collected by sponges as bacteria, unarmored cells, armored cells (fungi,
diatoms, etc.), and detritus. However, such plankters (2.5 to 13.5 p m diameter)
were an insignificant portion of the sponge diet. Almost all of the sponge’s
dietary, particulate organic carbon was composed of particles less than 1.5 pm.
The microscopically unresolveable, particulate organic carbon component “provides by far the major carbon source” (REISWIG,
1971 a, p. 582; REISWIC,1974).
Although Ophiothrix lineata ingested particles of a size theoretically suitable
as food particles for Callyspongia vaginalis, the majority of the particles utilized
by the sponge for food could not even be measured with the techniques
employed to examine the brittlestar diet. Therefore, the question of brittlestars
as parasites of sponges is, at present, unresolved. Although sponge spicules
were found in the brittlestar stomach contents, they also were found in the
siphon samples from the surface of the sponge and can be assumed to be part of
the sediment. Identifiable pieces of sponge tissue were not found in the
brittlestar stomach contents, indicating that 0. lineata does not prey on C.
4. Speculation regarding
a cleaning symbiosis
The feeding activities of Ophiothrix lineatn may benefit Callyspongia vnginnlis.
As the brittlestars feed, the incurrent filtering surface of the sponge is cleaned,
and this may promote greater pumping efficiency. There is no question that
pumping efficiency is of primary importance to sponges. Vital activities of
sponges such as feeding, respiration, and reproduction all depend on unob& FLECHSIG,
1979). Sponges survive in
structed flow of water (GERRODETTE
plankton-poor tropical waters by virtue of their remarkably efficient filterfeeding activities. Thus, they cannot afford to reduce their pumping rates for
extended periods of time (REISWIG,1971a, b; 1974).
The amount of sediment in suspension can limit distribution of :,ponges
(BAKUS,1968). Some demosponges are excluded from low-turbulence environments because they cannot maintain the sediment-free incurrent surfaces necessary for adequate pumping rates (REISWIG,1971a, 1974). For instance, the
is more sensitive to suspended sediments
sponge Verongia lacunosa (LAMARCK)
& FLECHthan any other filter-feeding organism previously tested (GERRODETTE
SIG, 1979).
Sponges are not without means of cleansing themselves. REISWIG( 1971a)
indicated that amoebocytes in the inhalent aquiferous system, capable of
capturing 2-5 pm particles, must operate continuously to prevent occlusion of
the aquiferous system by suspended particles. Sponges also employ reorganization of subdermal canals and sloughing of particles trapped in sponge mucus for
self-cleansing (REISWIG,1971a).
Callyspongia vaginalis commonly occurs in sandy lagoons (RAmALL &
1968). In such habitats it would likely be exposed to relatively heavy
sedimentation. Not all specimens of C. vuginalis at the study site had associated
brittlestars. Thus, a continuous association with Ophiothrix lineata is not
necessary for the survival of the sponge. However, the effectiveness of the
brittlestar in removing sediment coating the incurrent surface of the sponge has
been amply demonstrated. This is consistent with the hypothesis that the sponge
benefits from the activities of the brittlestar.
Whether the interaction between Ophiothrix lineata and Callysporigia vaginalis (or other brittlestars and sponges) is truly mutualistic remains to be
determined. It may be a facultative relationship (of mutual benefit) rather than
obligate mutualism (where both partners are dependent on each other). It
would be valuable to evaluate directly the pumping rate of Callyspongia
vaginalis with and without associated Ophiothrix lineata. However, LEWIS
(1982) has shown that the pumping behavior of C. vaginalis is difficult to record.
Certainly, reliable information on the pumping behavior and growth rates of
sponges with and without associated brittlestars will be of the utmost inlerest in
determining the true nature of sponge-brittlestar associations.
Brittlestar-sponge symbiosis
1. Large specimens of Ophiothrix Zineata are concealed in the tubes of CaZlyspongiu vaginafis during the day. At night the brittlestars sweep their arms
across the outer surface of the sponge as they feed, simultaneously cleaning the
sponge’s inhalent surface.
2. Ophiothrix lineata unselectively ingests detritus (and occassionally, microscopic organisms). Most of these particles are larger than the microscopically
unresolvable material utilized as food by sponges.
3. Diurnal fishes such as wrasses, parrotfish and porgies attack 0. Zineata
placed outside C. vaginalis, but not those dwelling inside C. vaginalis. Predation
on brittlestars was not detected at night. Apparently, the nocturnal activity of
the brittlestars is a predator avoidance strategy.
4. It is hypothesized that the brittlestar-sponge relationship is mutualistic.
Callyspongia vaginafis provides food and a refuge from predation for 0. lineata,
and it is suggested that the pumping efficiency of the sponge may be enhanced
by the feedingkleaning activity of the brittlestar.
The analysis of behavior using elapsed-time cinematography was possible with the generous loan of
camera and strobe equipment by its inventor, Dr. HAROLD
invaluable as a dive buddy, collector, keen observer, and skilled technical assistant. Mrs. LirrMAN
graciously provided Fig. 2 and Dr. GEORGE
contributed Fig. 3 for the color plate in this
advised and assisted with cinematography. Smithsonian voluntcers, Mr.
and Mr. GEORGE
GO patiently analysed clapsed-time films for
brittlestar activity patterns and sponge clearance rates. Mrs. BLEYLER
and another volunteer, Mrs.
measured ophiuroids for size and collected data on regeneration. Mrs. SANDY
volunteered to measure camera-lucida tracings of microscopic particles. Dr. LEE-ANNHAYEKand
provided advice on, and assistance with, statistical analyses. I availed myself of Dr.
knowledge of sponge biology, and he and Drs. DAVIDPAWSON
and Mr. JOHNMILLERprovided helpful criticism which improved the manuscript. To all these
colleagues, and many helpful friends in Belize, I am indebted and most grateful. Funding for this
study was provided through the E. R. FENNIMORE
Fund of the Smithsonian Institution, by
the Secretary’s Fluid Research Fund (Smithsonian Institution), and from an Exxon grant to Dr.
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